Primary Device ID | D9491120210 |
NIH Device Record Key | b3d822bc-7c82-4a45-b46e-d6233edf24ef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bioclear Diamond Wedge |
Version Model Number | Medium |
Company DUNS | 059020838 |
Company Name | Bioclear Matrix Systems |
Device Count | 50 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D9491120210 [Unit of Use] |
HIBCC | D949112021021 [Primary] |
HIBCC | D949112021041 [Primary] |
HIBCC | D949112021081 [Primary] |
HIBCC | D949112021101 [Primary] |
HIBCC | D949112021161 [Primary] |
HIBCC | D949112021500BG1 [Primary] |
HIBCC | D949112021501 [Primary] |
HIBCC | D949112021503 [Primary] |
HIBCC | D94911202150BG1 [Primary] |
EJB | Handle, Instrument, Dental |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-15 |
Device Publish Date | 2023-08-07 |
D9491120510 | Plastic wedge used in dental restorations. |
D9491120410 | Plastic wedge used in dental restorations. |
D9491120310 | Plastic wedge used in dental restorations. |
D9491120210 | Plastic wedge used in dental restorations. |
D949112011501 | Plastic wedge used in dental restorations. |
D9491120110 | Plastic wedge used in dental restorations. |